broadinstitute / gnomad-browserLinks
Explore gnomAD datasets on the web
☆83Updated this week
Alternatives and similar repositories for gnomad-browser
Users that are interested in gnomad-browser are comparing it to the libraries listed below
Sorting:
- Hail helper functions for the gnomAD project and Translational Genomics Group☆96Updated this week
- ☆69Updated this week
- Documentation and description of AWS iGenomes S3 resource.☆114Updated 7 months ago
- Plugins for the Ensembl Variant Effect Predictor (VEP)☆153Updated last week
- simple comparison of snakemake, nextflow and cromwell/wdl☆49Updated 4 years ago
- NGS-pipe: next-generation sequencing pipelines for precision oncology☆112Updated 6 years ago
- IGV Web App☆124Updated this week
- WashU Epigenome Browser☆73Updated 3 months ago
- A modular annotation tool for genomic variants☆125Updated last month
- ☆82Updated 6 years ago
- GTEx Visualizations☆64Updated 4 years ago
- Copy number vaiation detection from SNP arrays☆93Updated last year
- Workflows for converting between sequence data formats☆38Updated 3 years ago
- This repo provides tools to convert ClinVar data into a tab-delimited flat file, and also provides that resulting tab-delimited flat file…☆127Updated 5 years ago
- a Medical Genetics Sequence Analysis Pipeline☆83Updated this week
- Open workflow definitions for genomic analysis from MGI at WUSM.☆105Updated 3 weeks ago
- dbSNP☆137Updated last year
- SeqMonk NGS visualisation and analysis tool☆49Updated 3 weeks ago
- integrated RNA-seq Analysis Pipeline☆84Updated 6 years ago
- ☆62Updated 8 years ago
- This repo has been archived, these workflows are still available in the GATK repository under the scripts directory. The workflows are al…☆78Updated 5 years ago
- A Python package for pharmacogenomics (PGx) research☆75Updated 5 months ago
- A Python-based EGA download client☆101Updated 9 months ago
- Educational materials for learning WDL☆126Updated last year
- Extensible specification for representing and uniquely identifying biological sequence variation☆90Updated 3 months ago
- Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing☆133Updated 5 years ago
- Somatic copy number analysis using WGS paired end wholegenome sequencing☆72Updated 4 years ago
- TADbit is a complete Python library to deal with all steps to analyze, model and explore 3C-based data. With TADbit the user can map FAST…☆105Updated last month
- Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data☆85Updated 2 weeks ago
- TransVar - multiway annotator for precision medicine☆126Updated 2 years ago